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Merck

PHR1540

Supelco

Letrozol

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(e):

Letrozol, 4,4′-(1H-1,2,4-Triazol-1-ylmethylen)-bisbenzonitril

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About This Item

Empirische Formel (Hill-System):
C17H11N5
CAS-Nummer:
Molekulargewicht:
285.30
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

certified reference material
pharmaceutical secondary standard

Qualitätsniveau

Agentur

traceable to Ph. Eur. Y0000685
traceable to USP 1356971

API-Familie

letrozole

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

pkg of 1 g

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

pharmaceutical (small molecule)

Format

neat

Lagertemp.

2-30°C

SMILES String

N#CC(C=C1)=CC=C1C(N2C=NC=N2)C3=CC=C(C#N)C=C3

InChI

1S/C17H11N5/c18-9-13-1-5-15(6-2-13)17(22-12-20-11-21-22)16-7-3-14(10-19)4-8-16/h1-8,11-12,17H

InChIKey

HPJKCIUCZWXJDR-UHFFFAOYSA-N

Angaben zum Gen

human ... CYP19A1(1588)

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Allgemeine Beschreibung

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Letrozole is used for the treatment of breast cancer in hormone-dependent postmenopausal patients. The drug works by blocking the synthesis of estrogen, a causative agent for cancer.

Anwendung

Letrozole may be used as a pharmaceutical reference standard for the determination of the analyte in biological/environmental samples and pharmaceutical formulations by various chromatography techniques.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Biochem./physiol. Wirkung

Letrozol ist ein nicht-steroidaler Aromatase-Inhibitor der dritten Generation. Es ist ein kompetitiver Inhibitor des Aromatase Enzymsystems und verhindert so die Umwandlung von Androgenen zu Östrogenen. Letrozol hemmt Aromatase durch kompetitive Bindung an das Häm der Cytochrom-P450-Untereinheit des Enzyms, was zu einer Abnahme der Östrogen-Biosynthese in allen Geweben führt.

Hinweis zur Analyse

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Sonstige Hinweise

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Fußnote

To see an example of a Certificate of Analysis for this material enter LRAA4186 in the slot below. This is an example certificate only and may not be the lot that you receive.

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Ähnliches Produkt

Piktogramme

Health hazard

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Repr. 2 - STOT RE 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

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Kunden haben sich ebenfalls angesehen

Rapid determination of letrozole, citalopram and their metabolites by high performance liquid chromatography-fluorescence detection in urine: Method validation and application to real samples
Rodriguez J, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 913, 12-18 (2013)
Determination of letrozole in tablet formulations by reversed phase high performance liquid chromatography
Ganesh M, et al.
Tropical Journal of Pharmaceutical Research, 9(5), 505-510 (2010)
Rapid quantitative analysis of letrozole, fluoxetine and their metabolites in biological and environmental samples by MEKC
Rodriguez?Flores, et al.
Electrophoresis, 30(4), 624-632 (2009)
Adina Dumitrescu et al.
Endocrinology, 155(12), 4774-4784 (2014-09-24)
We have previously shown that estrogen selectively suppresses growth of the fetal zone of the baboon fetal adrenal cortex, which produces the C19-steroid precursors, eg, dehydroepiandrosterone sulfate, which are aromatized to estrogen within the placenta. In the present study, we
Kelley M Kidwell et al.
Cancer, 120(16), 2403-2411 (2014-05-08)
Aromatase inhibitor (AI) therapy results in substantial survival benefits for patients with hormone receptor-positive breast cancer. The rates of poor adherence and discontinuation of AI therapy are high, primarily because of treatment-related toxicities like musculoskeletal pain. Although pain-related symptoms may

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